نتایج جستجو برای: pluripotency specific

تعداد نتایج: 1040520  

2017
Stoyan G Petkov Silke Glage Heiner Niemann

Mouse somatic cells can be reprogrammed to pluripotency by the ectopic expression of four pluripotency transcription factors, Oct4, Sox2, cmyc, and Klf4. Usually, silencing of the exogenous reprogramming factors is considered to be essential for complete reprogramming and differentiation. In the vast majority of studies, murine pluripotency transcription factor sequences have been used for the ...

Journal: :Cell 2016
Xiaodong Shu Duanqing Pei

Mouse embryonic stem cells (mESCs) are capable of unlimited proliferation without losing pluripotency. Scognamiglio et al. now reveal that Myc depletion shifts mESCs into a dormant state reminiscent of embryonic diapause in which pluripotency remains fully preserved, thus decoupling pluripotency from proliferative programs.

Journal: :Theriogenology 2012
Z Tancos C Nemes Z Polgar E Gocza N Daniel T A E Stout P Maraghechi M K Pirity P Osteil Y Tapponnier S Markossian M Godet M Afanassieff Z Bosze V Duranthon P Savatier A Dinnyes

Pluripotent stem cells have the capacity to divide indefinitely and to differentiate into all somatic cells and tissue lines. They can be genetically manipulated in vitro by knocking genes in or out, and therefore serve as an excellent tool for gene function studies and for the generation of models for some human diseases. Since 1981, when the first mouse embryonic stem cell (ESC) line was gene...

Journal: :National science review 2014
Hongjun Song Guo-Li Ming

Somatic cells from animals and humans can be reprogrammed into pluripotent stem cells by pluripotency factors. Hongkui Deng and colleagues discovered that pluripotency can also be induced with exogenous lineage specifiers via balancing competing differentiation forces. In a related study they achieved, for the first time, restoration of pluripotency in adult somatic cells using a chemical cockt...

2016
Junghyun Jo Sohyun Hwang Hyung Joon Kim Soomin Hong Jeoung Eun Lee Sung-Geum Lee Ahmi Baek Heonjong Han Jin Il Lee Insuk Lee Dong Ryul Lee

Spermatogonial stem cells (SSCs) can spontaneously dedifferentiate into embryonic stem cell (ESC)-like cells, which are designated as multipotent SSCs (mSSCs), without ectopic expression of reprogramming factors. Interestingly, SSCs express key pluripotency genes such as Oct4, Sox2, Klf4 and Myc. Therefore, molecular dissection of mSSC reprogramming may provide clues about novel endogenous repr...

2014
Stephen J. Roper Stephanie Chrysanthou Claire E. Senner Arnold Sienerth Stefano Gnan Alexander Murray Mitsuko Masutani Paulina Latos Myriam Hemberger

Embryonic stem (ES) cells are in a dynamic equilibrium of distinct functional states, characterized by the heterogeneous expression of critical pluripotency factors and regulated by a spectrum of reversible histone modifications. Maintenance of this equilibrium is a hallmark of pluripotency. Here we find that the ADP-ribosyltransferases Parp1 and Parp7 play a critical role in safeguarding this ...

2011
Thorold W. Theunissen Yael Costa Aliaksandra Radzisheuskaya Anouk L. van Oosten Fabrice Lavial Bertrand Pain L. Filipe C. Castro José C. R. Silva

Pluripotency is a developmental ground state that can be recreated by direct reprogramming. Establishment of pluripotency is crucially dependent on the homeodomain-containing transcription factor Nanog. Compared with other pluripotency-associated genes, however, Nanog shows relatively low sequence conservation. Here, we investigated whether Nanog orthologs have the capacity to orchestrate estab...

2011
Ana V. Sánchez-Sánchez Esther Camp José L. Mullor

To understand the molecular mechanisms that regulate the biology of embryonic stem cells (ESCs) it is necessary to study how they behave in vivo in their natural environment. It is particularly important to study the roles and interactions of the different proteins involved in pluripotency and to use this knowledge for therapeutic purposes. The recent description of key pluripotency factors lik...

Journal: :Cell stem cell 2016
Jin Zhang Sutheera Ratanasirintrawoot Sriram Chandrasekaran Zhaoting Wu Scott B Ficarro Chunxiao Yu Christian A Ross Davide Cacchiarelli Qing Xia Marc Seligson Gen Shinoda Wen Xie Patrick Cahan Longfei Wang Shyh-Chang Ng Supisara Tintara Cole Trapnell Tamer Onder Yuin-Han Loh Tarjei Mikkelsen Piotr Sliz Michael A Teitell John M Asara Jarrod A Marto Hu Li James J Collins George Q Daley

The RNA-binding proteins LIN28A and LIN28B play critical roles in embryonic development, tumorigenesis, and pluripotency, but their exact functions are poorly understood. Here, we show that, like LIN28A, LIN28B can function effectively with NANOG, OCT4, and SOX2 in reprogramming to pluripotency and that reactivation of both endogenous LIN28A and LIN28B loci are required for maximal reprogrammin...

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